A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468729



Internal ID21126282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83568501..83570600hg38UCSC Ensembl
chr11:83279544..83281643hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994375
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer